Hell Week
The first week at home with our newly diagnosed 23 month old
daughter was what I like to refer to as “hell week”. I guarantee it would have
tried the patience and endurance of any Marine. I cried, I begged, I wondered
what the heck my life was turning out to be. And I wasn’t even the one
diagnosed with type 1 diabetes! But
seriously, I would have had to check into a mental asylum if it had been much
longer than that infuriatingly long week. Why do you ask? My toddler’s tantrums should have been the
basis for the Exorcist. She could have taught fellow two year olds on how to
properly throw a temper tantrum worthy of an Oscar nomination. You could have
filmed it for a reality TV show on dysfunctional children with behavioral
issues.
I want to preface the following by saying I totally would
have done the same thing if I was two years old and had no understanding of
what was happening to me. I probably would’ve despised my parents for seemingly
torturing me 10+ times a day with needles galore and on top of that, waking me up
throughout the night leaving me feeling like a zombie. However, sympathizing
does not alleviate the totality of the stress of having to watch your two year
old throw herself on the ground and bang her head backwards. Hitting, biting,
kicking, & deafening screams. I actually worried that my neighbors would
think that we were abusing our child from the sounds that emanated from our
house. I worried about concussions from the throwing her head backwards on the
tile. She developed bruises from the insulin shots from kicking in the middle
of an injection. She ran from us when we tried to get blood for her glucose
checks. We woke up every 2-3 hours to check her blood at night to make sure she
wasn’t going low. A lack of sleep abounded in our family. Did I mention I was
4.5 months pregnant during this?
I felt like no one could understand. She was eating more
than a teenage boy to recover from the weight loss associated from the DKA
episode (at her diagnosis). To everyone else, she was handling it like a champ.
But…..She had a special resentment just for mommy during our long hours alone
together while daddy was at work. I had to figure out pretzel-like maneuvers to
get her into a manageable position to give her shots & check her blood. I
had calculators all over the place to double check my carb counts before I
could feed her. And did I mention that she wanted to be fed NOW. As in blood
curdling screaming that would last from the instant she felt a hunger cue
through the blood check, preparation, cooling, counting, plating, etc. Did I mention she was hungry ALL THE TIME. And
on a feeding schedule. With limited carb amounts. Let’s just say she ate a lot
of cheese and sugar-free jello that week.
I was terrified of making a mistake. We had the smallest
syringe available and had to fill it to one of the two smallest lines within
the syringe. There was: two types of insulin to possibly mix up; lancets to
deal with; sharps containers to pick up; organization of the buckets of
diabetes care items and education; writing down EVERYTHING.
Everything I had taken for granted was becoming my most
treasured memories. Easter approached right after diagnosis and all the other
kids got Easter candies. Except my child, who couldn’t have them. It was like a
giant pity-party at our house. Mourning for the childhood she should have had,
filled with cotton candy, Halloween treats, birthday cake, candied apples,
Sunday morning pancakes, and baking cookies with mom.
All kidding aside, you literally go through the 7 stages of grief: Shock & Denial – yep; Pain & Guilt – double check; Anger & Bargaining – oh ya; Depression, Reflection & Loneliness – yep; Upward Turn – this is the “getting a handle on my emotions” portion; Reconstruction & Working Through – this one took a couple of months; Acceptance & Hope – 6 months later I am here.)
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